IQVIA · 3 hours ago
Clinical Trial Manager I, IQVIA Biotech
Prescott, AZ
Full-time
Onsite
Mid Level
$68K/yr - $171K/yr
3+ years expIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. The Clinical Trial Manager I will be responsible for ensuring the clinical delivery of assigned projects in compliance with regulatory and customer requirements, managing project risks, and collaborating with clinical teams to achieve project milestones.
AnalyticsHealth CareLife Science
Responsibilities
Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans)
Accountable for meeting projects’ recruitment targets and ensuring appropriate recruitment strategies are in place
Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project’s lifecycle
Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues
Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work
Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management
Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements
Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings
Conduct regular team meetings and communicate appropriately to achieve objectives
Support professional development by providing feedback to clinical team line managers on performance relative to project tasks
May work as the sole Clinical Lead on projects with 1-2 service lines and single/few countries or alongside more senior Clinical Leads to deliver large, global trials
May attend site visits as applicable in support of project delivery
Qualification
Required
Bachelor's Degree in health care or other scientific discipline required
Requires 3 years clinical research/monitoring experience or equivalent combination of education, training and experience
Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Requires broad protocol knowledge and therapeutic knowledge
Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates
Requires basic understanding of project finances
Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e., International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct
Strong written and verbal communication skills including good command of English language
Problem solving skills
Planning, time management and prioritization skills
Ability to handle conflicting priorities
Attention to detail and accuracy in work
Results-oriented approach to work delivery and output
Good software and computer skills, including Microsoft Office applications including but not limited to Microsoft Word, Excel and PowerPoint
Ability to establish and maintain effective working relationships with coworkers, managers and clients
Ability to work across cultures and geographies with a high awareness and understanding of cultural differences
Ability to influence without authority
Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership)
Benefits
Incentive plans
Bonuses
Health and welfare and/or other benefits
Company
IQVIA
IQVIA provides analytics, compliance, and management solutions to the life sciences industry.
10001+ employees
H1B Sponsorship
IQVIA has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (134)
2024 (299)
2023 (263)
2022 (229)
2021 (208)
2020 (180)
Funding
Current Stage
Public CompanyTotal Funding
$3.5B2025-06-02Post Ipo Debt· $2B
2023-11-14Post Ipo Debt· $500M
2023-05-18Post Ipo Debt· $1B
Leadership Team
Chris Colapietro
Vice President, Customer Engagement
Jonathan Morris
VP & GM US Healthcare
Recent News
Sabin Vaccine Institute
2025-12-04
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